A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141765



Internal ID19261974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:94497266..94497330hg38UCSC Ensembl
Outerchr13:95149520..95149584hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993271
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141765
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer